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TargetPurine nucleoside phosphorylase
LigandBDBM50081806
Substrate/Competitorn/a
Meas. Tech.ChEMBL_162011 (CHEMBL764862)
IC50 37±n/a nM
Citation Yokomatsu, THayakawa, YSuemune, KKihara, TSoeda, SShimeno, HShibuya, S Synthesis and biological evaluation of 1,1-difluoro-2-(tetrahydro-3-furanyl)ethylphosphonic acids possessing a N9-purinylmethyl functional group at the ring. a new class of inhibitors for purine nucleoside phosphorylases. Bioorg Med Chem Lett9:2833-6 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Purine nucleoside phosphorylase
Name:Purine nucleoside phosphorylase
Synonyms:Inosine phosphorylase | Inosine-guanosine phosphorylase | NP | PNP | PNPH_HUMAN | Purine nucleoside phosphorylase (PNPase)
Type:Enzyme
Mol. Mass.:32119.53
Organism:Homo sapiens (Human)
Description:n/a
Residue:289
Sequence:
MENGYTYEDYKNTAEWLLSHTKHRPQVAIICGSGLGGLTDKLTQAQIFDYGEIPNFPRST
VPGHAGRLVFGFLNGRACVMMQGRFHMYEGYPLWKVTFPVRVFHLLGVDTLVVTNAAGGL
NPKFEVGDIMLIRDHINLPGFSGQNPLRGPNDERFGDRFPAMSDAYDRTMRQRALSTWKQ
MGEQRELQEGTYVMVAGPSFETVAECRVLQKLGADAVGMSTVPEVIVARHCGLRVFGFSL
ITNKVIMDYESLEKANHEEVLAAGKQAAQKLEQFVSILMASIPLPDKAS
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50081806
n/a
NameBDBM50081806
Synonyms:CHEMBL94920 | {1,1-Difluoro-2-[(3R,4S)-4-(6-oxo-1,6-dihydro-purin-9-ylmethyl)-tetrahydro-furan-3-yl]-ethyl}-phosphonic acid
TypeSmall organic molecule
Emp. Form.C12H15F2N4O5P
Mol. Mass.364.2419
SMILESOP(O)(=O)C(F)(F)C[C@H]1COC[C@@H]1Cn1cnc2c1nc[nH]c2=O
Structure
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